Beijing Research Institute of Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
J Hematol Oncol. 2023 Jul 31;16(1):87. doi: 10.1186/s13045-023-01485-7.
NEDDylation, a post-translational modification through three-step enzymatic cascades, plays crucial roles in the regulation of diverse biological processes. NEDD8-activating enzyme (NAE) as the only activation enzyme in the NEDDylation modification has become an attractive target to develop anticancer drugs. To date, numerous inhibitors or agonists targeting NAE have been developed. Among them, covalent NAE inhibitors such as MLN4924 and TAS4464 currently entered into clinical trials for cancer therapy, particularly for hematological tumors. This review explains the relationships between NEDDylation and cancers, structural characteristics of NAE and multistep mechanisms of NEDD8 activation by NAE. In addition, the potential approaches to discover NAE inhibitors and detailed pharmacological mechanisms of NAE inhibitors in the clinical stage are explored in depth. Importantly, we reasonably investigate the challenges of NAE inhibitors for cancer therapy and possible development directions of NAE-targeting drugs in the future.
泛素化修饰是通过三步酶级联反应进行的一种翻译后修饰,在调节多种生物过程中起着至关重要的作用。NEDD8-激活酶(NAE)作为泛素化修饰中的唯一激活酶,已成为开发抗癌药物的有吸引力的靶点。迄今为止,已经开发出许多针对 NAE 的抑制剂或激动剂。其中,共价 NAE 抑制剂,如 MLN4924 和 TAS4464,目前已进入癌症治疗的临床试验,特别是用于血液肿瘤。本文综述了泛素化修饰与癌症之间的关系、NAE 的结构特征以及 NAE 激活 NEDD8 的多步机制。此外,还深入探讨了发现 NAE 抑制剂的潜在方法以及 NAE 抑制剂在临床阶段的详细药理学机制。重要的是,我们合理地研究了 NAE 抑制剂在癌症治疗中的挑战以及未来 NAE 靶向药物的可能发展方向。